• Solid knowledge of Oncology therapeutic area and provide insight about oncology biomarker, Patients segment, diagnostic tests, hematologic and solid tumors.• Comprehensive and robust secondary research skills.• Strong analytical skills• Maintaining competitive clinical landscape of cancer through secondary research, analyzing, annotation & data curation of clinical data from Phase I to IV through web-based domains.• Perform end to end comparative analysis of clinical studies from clinical data summary, AEs, efficacy endpoints to upcoming milestone.• Do strategic planning of new task for successful execution, recognize high performance and reward accomplishments.• Monitored internal project and ensured completion should be on time. • Responsible for overseeing day-to-day operation by handling team queries, tasks delegations and set deadlines for new tasks.• Monitor team performance via spot check and report on metrics and participating in training and Maintain daily as well as weekly work tracker of team• Including my daily tasks I am participating in other activities like presentation of competitor’s profiles, organize team building activities, idea contests, monthly contests and social media engagement• Handling weekly reports of customers. Responsible and accountable for quality check as well as delivery of customer’s reports. • Highly proficient in the use of MS word, PowerPoint and Excel • Able to attend all type of calls via team or Zoom app• Do Benchmarking of clinical studies - Recruitment Rate (Median recruitment rate or Average recruitment rate)• Team Synergy Catalyst: Responsible for providing activities to all team leaders for cross communication• Involved in social media activities and handled social media post related to few products• Provides new ideas or epics for improvements of process or project• Handling internal project as per client requirement

• Data Analysis, Data Mining & Secondary Research • Carry out and supervise secondary market research in diverse domains and identify emerging trends• Strong analytical and decision making skills as per available data• Great knowledge of biomarker and personalized medicine• Ability to track data related to biomarker and drugs associations• Great biomarker analysis from all publication either from pubmed, conferences etc• Able to analyze biomarker association either sensitive or resistant on the basis of publication result• Able to do competitive analysis of the drugs related to biomarker area for oncology• Effectively and proactively communicate with team members and management• Strong mentor and QC skill• Competitive scientific meetings and literature coverage• Supervising, mentoring, training and management of juniors within the team • Database quality checks/assurance • Bio-pharmaceutical company coverage, analysis, making PPT, and presentation skills• Collect & analyze the information from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences, annual meetings (ASH, ASCO), Etc.• Handled conferences coverage• Handled Daily surveillance for top tumor types• Handled all request like regimen addition, alterations and drug addition with respective team• Good computer skills and skilled with Ms word, Ms PowerPoint, MS Excel, and Outlook• Able to quickly acquire working knowledge regarding a variety of scientific/medical fields• Strong interpersonal skills and the ability to be flexible in varying environment Roles & Responsibilities

Roles & Responsibilities• Carry out and supervise secondary market research in diverse domains and identify emerging trends• Collect and analyze the data related to diverse sector• Strong analytical and decision making skills as per available data• Able to do competitive analysis of the drugs • Able to write CSR as per ICH E3 guideline • Peer-review of TFLs and able to create Tables from listing and figures as per client requirement• Patients safety narrative (PSN)• Data integrity (DI) check• Academic writing like literature review through comprehensive searches in the PubMed and Google scholar and research article as per client requirement• Write references as per MLA, APA, Chicago, Harvard, and Vancouver style• Able to write articles and blogs-medical niche• Effectively and proactively communicate with team members and management• Able to generate effective tables and graphs and use of applicable Microsoft software • Give Training related to clinical trials (Phases, Drugs, Therapeutic areas, Clinical trial design, Accrual of the study etc) and searching technique to medical writing team members.• Meet project deadline always• Do quality check of the automatically scrapped conferences in the Confowiz software. Analysis of correct molecules/drugs/biomarkers/receptors/technology drugs/clinical trials in the conferences’ database• Great mentoring skills• Good computer skills and skilled with Ms word, Ms PowerPoint, MS Excel, and Outlook• Able to quickly acquire working knowledge regarding a variety of scientific/medical fields• Good knowledge of drug development process• Strong interpersonal skills and the ability to be flexible in varying environment Roles & Responsibilities

 I have worked as Medical Research ExecutionRoles & Responsibilities:• Collect & analyze the information about marketed & development stage products of Bio-Pharmaceutical companies including clinical trial data, regulatory information (approvals & filings of NDA, BLA etc), press release tracking & analysis, Deal-M&A (mergers & acquisitions), patent updates capture for products & companies from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences, annual meetings (ASH, ASCO), Etc.• Competitive scientific meetings and literature coverage • Preparation of a competitive landscape for drugs, devices and clinical • Supervising, mentoring, training and management of juniors within the team • Database quality checks/assurance • Bio-pharmaceutical company coverage • Data Analysis, Data Mining & Secondary Research • Drug pipeline tracking data (Phase I, II, III & IV) • Global Meeting/conference coverage • Scientific publication analysis of molecules/receptors/technology drugs/clinical trials • MOA and Clinical/Pre-clinical data evaluation • Clinical Trial Timing Benchmarking •Accessing, analyzing and interpretation from the research clinical data.